United States · FDA National Drug Code directory
Ciprofloxacin
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 68788-8136_e6e1419a-65f6-42a7-a4f9-67a2fdf7aa53
- Product NDC
- 68788-8136
- Form
- TABLET, FILM COATED
- Composition / generic term
- Ciprofloxacin Hydrochloride
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220203
- Source listing expiry
- 20261231
Source-listed ingredients
- CIPROFLOXACIN HYDROCHLORIDE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 TABLET, FILM COATED in 1 BOTTLE (68788-8136-0) · 68788-8136-0
- 14 TABLET, FILM COATED in 1 BOTTLE (68788-8136-1) · 68788-8136-1
- 20 TABLET, FILM COATED in 1 BOTTLE (68788-8136-2) · 68788-8136-2
- 30 TABLET, FILM COATED in 1 BOTTLE (68788-8136-3) · 68788-8136-3
- 10 TABLET, FILM COATED in 1 BOTTLE (68788-8136-8) · 68788-8136-8
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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